The Anspach Effort, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2126-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.

Product Classification:

Class II

Date Initiated: November 25, 2015

Date Posted: July 13, 2016

Recall Number: Z-2126-2016

Event ID: 73198

Reason for Recall:

Has the incorrect operating directions on the mode switch ring, i.e. its is labeled "FWD, LOCK, REV" instead of "ON, LOCK, ON".

Status: Terminated

Product Quantity: 20 hand pieces

Code Information:

Part Number 530.710, Serial Numbers 101066, 101067, 101068, 101069, 101070, 101071, 101072, 101073, 101074, 101075, 101076, 101077, 101078, 101079, 1011080, 101081, 101082, 101083, 101084, 101085

Distribution Pattern:

US Distribution to the state of : VA and Internationally to: Thailand and UK

Voluntary or Mandated:

Voluntary: Firm initiated